Literature DB >> 5704437

[Partial D-1 trisomy--a rare chromosome abnormality].

E Krüger, R Witkowski, U Piede.   

Abstract

Mesh：

Year:  1968        PMID： 5704437     DOI： 10.1007/bf00297727

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  18 in total

1.  RECIPROCAL (D;E) TRANSLOCATION: EUPLOID TRANSMISSION IN THREE GENERATIONS.

Authors:  B R MIGEON; W J YOUNG
Journal:  Bull Johns Hopkins Hosp       Date:  1964-11

2.  [MULTIPLE CONGENITAL MALFORMATIONS IN 2 SISTERS. POSSIBLE ASSOCIATION WITH A CHROMOSOME 22 ABNORMALITY. PRELIMINARY NOTE].

Authors:  J FREDERIC; Y MONARD; F BONNET; P DODINVAL
Journal:  Rev Med Liege       Date:  1964-04-15

3.  NORMAL-TRISOMY 13-15 MOSAICISM IN TWO INFANTS.

Authors:  A D BAIN; J INSLEY; D M DOUGLAS; I K GAULD; H A SCOTT
Journal:  Arch Dis Child       Date:  1965-08       Impact factor: 3.791

4.  Dermal patterns of 18 and D1 trisomics.

Authors:  I A UCHIDA; K PATAU; D W SMITH
Journal:  Am J Hum Genet       Date:  1962-12       Impact factor: 11.025

5.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal:  Exp Cell Res       Date:  1960-09       Impact factor: 3.905

6.  Multiple congenital anomaly caused by an extra autosome.

Authors:  K PATAU; D W SMITH; E THERMAN; S L INHORN; H P WAGNER
Journal:  Lancet       Date:  1960-04-09       Impact factor: 79.321

7.  [Chromosome anomalies caused by surplus (trisomies) and age of the mother].

Authors:  W Lenz; R A Pfeiffer; W Tünte
Journal:  Dtsch Med Wochenschr       Date:  1966-07-15       Impact factor: 0.628

8.  A family with balanced D1-Cs-translocation carriers and unbalanced offspring.

Authors:  G R Stalder; E M Buhler; G Gadola; R Widmer; F Freuler
Journal:  Humangenetik       Date:  1964

9.  Translocation in trisomy D syndrome. A case of a probable D/18 translocation.

Authors:  A P Craig; L Luzzatti
Journal:  J Pediatr       Date:  1967-02       Impact factor: 4.406

10.  Familial transmission of a translocation between two non-homologous large acrocentric chromosomes. Clinical, cytogenetic and autoradiographic studies.

Authors:  P Jacobsen; M Mikkelsen; A Froland; A Dupont
Journal:  Ann Hum Genet       Date:  1966-05       Impact factor: 1.670
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  8 in total

1.  Dermatoglyphic findings in 54 triple-X females and a review of some general principles applying to the soles in sex chromosome aneuploidy.

Authors:  P Saldaña-Garcia
Journal:  J Med Genet       Date:  1975-06       Impact factor: 6.318

2.  Supernumerary small ring chromosome.

Authors:  J J Hoo; C Forster; I Kindermann; B Zabel; S Hansen
Journal:  Humangenetik       Date:  1974

3.  Partial trisomy 13: karyotype 46,XY,-6, plus t(13q,6q).

Authors:  J P Fryns; E Eggermont; H Verresen; H van den Berghe
Journal:  Humangenetik       Date:  1974-01-22

4.  A chromosome 13q+ in a patient with characteristics of the trisomy 13 syndrome.

Authors:  H Hoehn; U Wolf; H Schumacher; H Wehinger
Journal:  Humangenetik       Date:  1971

5.  The aetiology of the cat eye syndrome reconsidered.

Authors:  G Guanti
Journal:  J Med Genet       Date:  1981-04       Impact factor: 6.318

Review 6.  [Cat-eye syndrome. Clinical and cytogenetical differentialdiagnosis (author's transl)].

Authors:  J Kunze; M Tolksdorf; H R Wiedemann
Journal:  Humangenetik       Date:  1975

7.  Proximal trisomy 13. A family with balanced reciprocal translocation t(8;13) in seven members and Robertsonian translocation t(13;14) in three members.

Authors:  S Gilgenkrantz; C Defeche; S Stehlin; M J Gregoire
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

8.  Trisomy 22. Two new cases and delineation of the phenotype.

Authors:  V B Penchaszadeh; R Coco
Journal:  J Med Genet       Date:  1975-06       Impact factor: 6.318
  8 in total

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